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首页> 外文期刊>European Journal of Plant Pathology >An enrichment microsphere immunoassay for the detection of Pectobacterium atrosepticum and Dickeya dianthicola in potato tuber extracts
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An enrichment microsphere immunoassay for the detection of Pectobacterium atrosepticum and Dickeya dianthicola in potato tuber extracts

机译:一种富集微球免疫分析法,用于检测马铃薯块茎提取物中的土壤杆菌和迪卡迪克菌

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摘要

An enrichment microsphere immunoassay (MIA) was developed, based on the Luminex xMAP? technology, for the simultaneous (duplex) detection of Pectobacterium atrosepticum (former name Erwinia carotovora subsp. atroseptica) (Pca) and Dickeya dianthicola (former name Erwinia chrysanthemi) (Dcd) in potato plant extracts. Target bacteria in the extracts were enriched for 48 h in a semi-selective broth containing polypectate under low oxygen conditions. Samples were subsequently incubated with antibody-coated colour-coded microspheres (beads) and with secondary antibodies conjugated with Alexa Fluor? 532, a reporter dye. Samples were analyzed with the Luminex analyzer, in which one laser identified each microsphere and another laser the reporter dye conjugated to the secondary antibodies. The assay required minimal sample preparation, could be completed in 1 h, was performed in 96 wells microtitreplates and required no wash steps. The limit of detection for the duplex enrichment MIA was 100–1000 cfu ml?1, which was a hundred times lower than of an enrichment-ELISA. Without enrichment, the sensitivity of MIA and ELISA was largely similar and ranged between 106 and 107 cells ml?1. No difference in sensitivity was found between a MIA in a single or duplex format. In a comparative test with non-infected potato plant extracts and extracts from plants infected with Pca or Dcd, results of the enrichment MIA correlated well with those of the enrichment ELISA and enrichment PCR. These results indicate that MIA can be reliably used for multiplex detection of soft rot Enterbacteriaceae in crude potato plant extracts. The technology is an attractive and cost-effective alternative to other detection methods, including ELISA.
机译:基于Luminex xMAP?开发了一种富集微球免疫测定(MIA)。技术,用于同时(双工)检测马铃薯植物提取物中的土壤杆菌(原名欧文氏菌亚种)(Pca)和狄氏菌(原名欧文氏菊)(Dcd)。在低氧条件下,将提取物中的目标细菌在含有聚果胶的半选择肉汤中富集48小时。随后将样品与涂有抗体的颜色编码的微球(珠子)以及与AlexaFluor®共轭的二抗一起孵育。 532,记者染料。用Luminex分析仪分析样品,其中一个激光识别每个微球,另一个激光将报告染料偶联到第二抗体上。该测定所需的样品制备量最少,可以在1小时内完成,在96孔微量滴定板中进行,并且无需洗涤步骤。双链富集MIA的检出限为100–1000 cfu ml?1 ,比富集ELISA低100倍。在不富集的情况下,MIA和ELISA的敏感性基本相似,范围在106 和107 ml ml?1 之间。在单个或双工格式的MIA之间,在灵敏度上未发现差异。在未感染的马铃薯植物提取物和受Pca或Dcd感染的植物提取物中的比较试验中,富集MIA的结果与富集ELISA和富集PCR的结果具有很好的相关性。这些结果表明,MIA可以可靠地用于粗马铃薯植物提取物中软腐肠杆菌科的多重检测。该技术是包括ELISA在内的其他检测方法的一种有吸引力且具有成本效益的替代方法。

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